438 Results for "

Adenosine Receptor

" in MedChemExpress (MCE) Product Catalog:
Products (438)

438 Results for "Adenosine Receptor" in MCE Product Catalog:

22
22 Publications Verification
Cat. No.: HY-A0181
CAS No.: 61-19-8
Synonyms: AMP
Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction .
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22
22 Publications Verification
Cat. No.: HY-A0181A
CAS No.: 18422-05-4
Synonyms: 5'-AMP monohydrate
Adenosine 5'-monophosphate monohydrate is an adenosine A1 receptor agonist. Adenosine 5'-monophosphate monohydrate has significant antiviral activity against HSV-1 and HSV-2 .
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22
22 Publications Verification
Cat. No.: HY-W011012
CAS No.: 4578-31-8
Adenosine 5'-monophosphate disodium is an orally active purine nucleotide, and participates in ATP metabolism. Adenosine 5'-monophosphate disodium is also a ligand for adenosine 2B receptor. Adenosine 5'-monophosphate disodium can activate AMPK in skeletal muscle, and ameliorates insulin resistance and impaired glucose metabolism. Adenosine 5'-monophosphate disodium can be used for research of diabetes .
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18
18 Cited Publications
Cat. No.: HY-19533
CAS No.: 160098-96-4
Target:  

Adenosine Receptor

Research Areas:  

Cancer

SCH 58261 is a potent, selective and competitive antagonist of adenosine A2A receptor with an IC50 of 15 nM, and displays 323-, 53- and 100-fold more selective for A2A receptor than A1, A2B, and A3 receptors, respectively .
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18
18 Cited Publications
Cat. No.: HY-B0228
CAS No.: 58-61-7
Synonyms: Adenine riboside; D-Adenosine
Adenosine (Adenine riboside), a ubiquitous and BBB-permeable endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation .
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16
16 Cited Publications
Cat. No.: HY-N0092
CAS No.: 58-63-9
Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors .
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16
16 Cited Publications
Cat. No.: HY-10888
CAS No.: 155270-99-8
Purity:  99.89%
Synonyms: KW-6002
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

Istradefylline is a very potent, selective and orally active adenosine A2A receptor antagonist with Ki of 2.2 nM in experimental models of Parkinson's disease.
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16
16 Cited Publications
Cat. No.: HY-19532
CAS No.: 139180-30-6
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease Cancer

ZM241385 is a potent, high affinity and selective adenosine A2a receptor (A2AR) antagonist with a Ki value of 1.4 nM .
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14
14 Cited Publications
Cat. No.: HY-13201
CAS No.: 120225-54-9
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

CGS 21680 is a selective adenosine A2A receptor agonist, with a Ki of 27 nM.
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14
14 Cited Publications
Cat. No.: HY-13201A
CAS No.: 124431-80-7
Purity:  99.70%
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

CGS 21680 Hydrochloride is a selective adenosine A2A receptor agonist with a Ki of 27 nM.
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13
13 Cited Publications
Cat. No.: HY-B0140
CAS No.: 317-34-0
Aminophylline is a competitive phosphodiesterase 3/4 (PDE3/4) inhibitor. Aminophylline also acts as an adenosine receptor antagonist. Aminophylline elevates intracellular cAMP levels via competitive inhibition of PDE3 and PDE4, antagonizes adenosine A1 receptor (ADORA1), regulates intracellular calcium signaling and synaptic vesicle cycling, upregulates the PPAR signaling pathway, and downregulates glutamatergic synaptic pathways simultaneously. Aminophylline can be used in research related to major depressive disorder, epilepsy, and chronic obstructive pulmonary disease (COPD) .
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13
13 Cited Publications
Cat. No.: HY-15424
CAS No.: 24386-93-4
Purity:  99.64%
Synonyms: NSC 113939; 5-ITu
Target:  

Adenosine Kinase

Research Areas:  

Cancer

5-Iodotubercidin (NSC 113939), an ATP mimetic, is a potent adenosine kinase inhibitor with an IC50 of 26 nM. 5-Iodotubercidin (NSC 113939) initiates glycogen synthesis in isolated hepatocytes by causing inactivation of phosphorylase and activation of glycogen synthase. 5-Iodotubercidin (NSC 113939) also inhibits CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2, PKC and Haspin .
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13
13 Cited Publications
Cat. No.: HY-B0809
CAS No.: 58-55-9
Synonyms: 1,3-Dimethylxanthine; Theo-24
Theophylline (1,3-Dimethylxanthine) is a potent phosphodiesterase (PDE) inhibitor, adenosine receptor antagonist, and histone deacetylase (HDAC) activator. Theophylline (1,3-Dimethylxanthine) inhibits PDE3 activity to relax airway smooth muscle. Theophylline (1,3-Dimethylxanthine) has anti-inflammatory activity by increase IL-10 and inhibit NF-κB into the nucleus. Theophylline (1,3-Dimethylxanthine) induces apoptosis. Theophylline (1,3-Dimethylxanthine) can be used for asthma and chronic obstructive pulmonary disease (COPD) research .
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11
11 Cited Publications
Cat. No.: HY-B0809A
CAS No.: 5967-84-0
Synonyms: 1,3-Dimethylxanthine monohydrate; Theo-24 monohydrate
Theophylline (1,3-Dimethylxanthine) monohydrate is a potent phosphodiesterase (PDE) inhibitor, adenosine receptor antagonist, and histone deacetylase (HDAC) activator. Theophylline (1,3-Dimethylxanthine) monohydrate inhibits PDE3 activity to relax airway smooth muscle. Theophylline (1,3-Dimethylxanthine) monohydrate has anti-inflammatory activity by increase IL-10 and inhibit NF-κB into the nucleus. Theophylline (1,3-Dimethylxanthine) monohydrate induces apoptosis. Theophylline (1,3-Dimethylxanthine) monohydrate can be used for asthma and chronic obstructive pulmonary disease (COPD) research .
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10
10 Cited Publications
Cat. No.: HY-14917
CAS No.: 544417-40-5
Purity:  99.62%
Synonyms: BAY 68-4986
Target:  

Adenosine Receptor

Research Areas:  

Cardiovascular Disease

Capadenoson is a selective agonist of adenosine-A1 receptor.
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9
9 Cited Publications
Cat. No.: HY-129393
CAS No.: 2239273-34-6
Purity:  99.67%
Synonyms: AB928
Target:  

Adenosine Receptor

Research Areas:  

Inflammation/Immunology Cancer

Etrumadenant (AB928) is an orally bioavailable, selective dual adenosine receptor (A2aR/A2bR) antagonist. Etrumadenant relieves adenosine-mediated immune suppression. Etrumadenant has immunomodulatory and antitumor activities .
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9
9 Cited Publications
Cat. No.: HY-W010791
CAS No.: 20398-34-9
Target:  

Endogenous Metabolite

Research Areas:  

Others

Adenosine 5'-diphosphate sodium salt is a nucleoside diphosphate and the product of ATP dephosphorylation by ATPases. Adenosine 5'-diphosphate sodium salt induces human platelet aggregation and inhibits stimulated adenylate cyclase through its action on P2T-purinergic receptors .
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9
9 Cited Publications
Cat. No.: HY-101978
CAS No.: 1202402-40-1
Purity:  99.85%
Synonyms: CPI-444; V81444
Target:  

Adenosine Receptor

Research Areas:  

Cancer

Ciforadenant (CPI-444) is a potent, orally active and selective adenosine A2A receptor (A2AR) antagonist, which induces antitumor responses .
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9
9 Cited Publications
Cat. No.: HY-100937
CAS No.: 102146-07-6
Purity:  99.96%
Synonyms: PD 116948
Target:  

Adenosine Receptor

Research Areas:  

Cardiovascular Disease

DPCPX (PD 116948), a xanthine derivative, is a highly potent and selective Adenosine A1 receptor antagonist, with a Ki of 0.46 nM in 3H-CHA binding to A1 receptors in rat whole brain membranes .
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9
9 Cited Publications
Cat. No.: HY-13591
CAS No.: 152918-18-8
Purity:  99.01%
Synonyms: IB-MECA; CF-101
Piclidenoson (IB-MECA) is a first-in-class, orally active and selective A3 adenosine receptor (A3AR) agonist. Piclidenoson exhibits antiproliferative effect and induces apoptosis in different cancer cell types like melanoma, leukemia. Piclidenoson can be used for the research of autoimmune inflammatory diseases and COVID-19 .
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